SULFOMETURON-METHYL

Details

Stereochemistry	ACHIRAL
Molecular Formula	C15H16N4O5S
Molecular Weight	364.376
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC(=O)C1=C(C=CC=C1)S(=O)(=O)NC(=O)NC2=NC(C)=CC(C)=N2

InChI

InChIKey=ZDXMLEQEMNLCQG-UHFFFAOYSA-N

InChI=1S/C15H16N4O5S/c1-9-8-10(2)17-14(16-9)18-15(21)19-25(22,23)12-7-5-4-6-11(12)13(20)24-3/h4-8H,1-3H3,(H2,16,17,18,19,21)

HIDE SMILES / InChI

Molecular Formula	C15H16N4O5S
Molecular Weight	364.376
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Inhibitors of branched-chain amino acid biosynthesis as potential antituberculosis agents.	1998 Oct	9818746
Simultaneous determination of binary mixtures of sulfonylurea herbicides in water by first-derivative photochemically induced spectrofluorimetry.	2001 Nov-Dec	11767141
Molecular analysis of the acetolactate synthase gene of Chlamydomonas reinhardtii and development of a genetically engineered gene as a dominant selectable marker for genetic transformation.	2002 Jan	12060231
Evolution of herbicide resistance in weeds: initial frequency of target site-based resistance to acetolactate synthase-inhibiting herbicides in Lolium rigidum.	2002 Jan	11813100
Isoleucine starvation caused by sulfometuron methyl in Salmonella typhimurium measured by translational frameshifting.	2002 Mar	11882705
Stable chloroplast transformation of the unicellular red alga Porphyridium species.	2002 May	12011332
Slow-release formulations of sulfometuron incorporated in micelles adsorbed on montmorillonite.	2002 May 8	11982412
Sulfometuron incorporation in cationic micelles adsorbed on montmorillonite.	2002 May 8	11982411
Acetohydroxyacid synthase from Mycobacterium avium and its inhibition by sulfonylureas and imidazolinones.	2003 Jun 26	12818195
Trace analysis of sulfonylurea herbicides in water by on-line continuous flow liquid membrane extraction--C18 precolumn liquid chromatography with ultraviolet absorbance detection.	2003 May 2	12800919
New small-molecule synthetic antimycobacterials.	2005 Jun	15917508
Sulfometuron resistance as a genetic marker for yeast populations in wine fermentations.	2005 Sep 21	16159170
Pesticide mixtures, endocrine disruption, and amphibian declines: are we underestimating the impact?	2006 Apr	16818245
Unraveling condition specific gene transcriptional regulatory networks in Saccharomyces cerevisiae.	2006 Mar 21	16551355
Transcriptional regulation by protein kinase A in Cryptococcus neoformans.	2007 Mar	17367210
Identification of the catalytic subunit of acetohydroxyacid synthase in Haemophilus influenzae and its potent inhibitors.	2007 Oct 1	17718999
Inference of protein complex activities from chemical-genetic profile and its applications: predicting drug-target pathways.	2008 Aug 29	18769708
A kinetic platform for in silico modeling of the metabolic dynamics in Escherichia coli.	2010	21918631
Predicting the pathway involved in post-translational modification of elongation factor P in a subset of bacterial species.	2010 Jan 13	20070887
Sulfonylureas have antifungal activity and are potent inhibitors of Candida albicans acetohydroxyacid synthase.	2013 Jan 10	23237384

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 07:10:51 GMT 2023` Edited by `admin` on `Sat Dec 16 07:10:51 GMT 2023`
Record UNII	JLY5D60J1A
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

SULFOMETURON-METHYL

Common Name

English

OUST

Brand Name

English

SULFOMETURON METHYL ESTER

Common Name

English

2-(3-(4,6-DIMETHYLPYRIMIDIN-2-YL)UREIDOSULFONYL)BENZOIC ACID METHYL ESTER

Systematic Name

English

SULFOMETURON-METHYL [HSDB]

Common Name

English

DPX-5648

Code

English

SULFOMETURON-METHYL [ISO]

Common Name

English

SULFOMETURON-METHYL [MI]

Common Name

English

Code System Code Type Description

PUBCHEM

52997